US20230405687A1 - Cutting tool - Google Patents

Cutting tool Download PDF

Info

Publication number
US20230405687A1
US20230405687A1 US18/018,890 US202218018890A US2023405687A1 US 20230405687 A1 US20230405687 A1 US 20230405687A1 US 202218018890 A US202218018890 A US 202218018890A US 2023405687 A1 US2023405687 A1 US 2023405687A1
Authority
US
United States
Prior art keywords
layer
less
unit layer
cutting tool
unit
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US18/018,890
Inventor
Yuta Suzuki
Shinya Imamura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Electric Hardmetal Corp
Original Assignee
Sumitomo Electric Hardmetal Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Electric Hardmetal Corp filed Critical Sumitomo Electric Hardmetal Corp
Assigned to SUMITOMO ELECTRIC HARDMETAL CORP. reassignment SUMITOMO ELECTRIC HARDMETAL CORP. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SUZUKI, YUTA, IMAMURA, SHINYA
Publication of US20230405687A1 publication Critical patent/US20230405687A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • C23C30/005Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B27/00Tools for turning or boring machines; Tools of a similar kind in general; Accessories therefor
    • B23B27/14Cutting tools of which the bits or tips or cutting inserts are of special material
    • B23B27/148Composition of the cutting inserts
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/042Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material including a refractory ceramic layer, e.g. refractory metal oxides, ZrO2, rare earth oxides
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/044Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material coatings specially adapted for cutting tools or wear applications
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/40Coatings including alternating layers following a pattern, a periodic or defined repetition
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/40Coatings including alternating layers following a pattern, a periodic or defined repetition
    • C23C28/42Coatings including alternating layers following a pattern, a periodic or defined repetition characterized by the composition of the alternating layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23BTURNING; BORING
    • B23B2228/00Properties of materials of tools or workpieces, materials of tools or workpieces applied in a specific manner
    • B23B2228/10Coatings
    • B23B2228/105Coatings with specified thickness

Definitions

  • the present disclosure relates to a cutting tool.
  • Patent Literature 1 and Patent Literature 2 Conventionally, coatings that coat a surface of a base material made of cemented carbide, sintered cubic boron nitride and the like have been developed in order to improve performance of cutting tools (for example, Patent Literature 1 and Patent Literature 2).
  • the cutting tool of the present disclosure is a cutting tool comprising a base material and a coating arranged on the base material, wherein
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum arid boron is 50% or more in the first layer.
  • FIG. 2 is a view explaining a measurement region when measuring the diameter of the largest inscribed circle of a crystal grain of a first layer.
  • FIG. 3 is a schematic view explaining a method for measuring the diameter of the largest inscribed circle of a crystal grain of a first layer, a schematic view illustrating a bright field image of a measurement field of view.
  • FIG. 3 A is a view explaining positional relationship between a crystal grain, a first unit layer and a second unit layer.
  • FIG. 4 is a schematic cross-sectional view illustrating an example of the configuration of a film deposition apparatus.
  • FIG. 5 is a schematic cross-sectional view illustrating an example of the configuration of a film deposition apparatus.
  • the cutting tool of the present disclosure can have a long tool life.
  • the coating includes a first layer
  • the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.
  • the cutting tool of the present disclosure can have a long tool life.
  • the first layer is composed of a plurality of crystal grains
  • the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
  • the microstructure of the first layer is dense, thereby improving wear resistance and chipping resistance of the cutting tool.
  • a half width of a diffraction peak derived from (200) plane of a cubic crystal is preferably 0.2° or more and 2.0° or less.
  • the proportion of the cubic crystal structure in the first layer is high, thereby enabling high hardness of the first layer, which results in improvements in the wear resistance of the cutting tool.
  • the cutting tool can have excellent wear resistance as well as chipping resistance, enabling further improvements in its tool life.
  • Compounds and the like when represented by chemical formulae in the present disclosure shall include all conventionally known atomic ratios as long as the atomic ratios thereof and not particularly limited, and should not necessarily be limited only to those in their stoichiometric ranges.
  • the ratio of the number of atoms constituting TiN includes all conventionally known atomic ratios.
  • any one numerical value described for the lower limit and any one numerical value described for the upper limit shall also be disclosed.
  • a1 or more, b1 or more, or c1 or more is described as the lower limit, and a2 or less, b2 or less, and c2 or less as the upper limit, a1 or more and a2 or less, a1 or more and b2 or less, a1 or more and c2 or less, and b1 or more and a2 or less, b1 or more and to b2 or less, b1 or more and c2 or less, c1 or more and a2 or less, and c1 or more and b2 or less, and c1 or more and c2 or less, shall be disclosed.
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.
  • the cutting tool of the present disclosure can have a long tool life. The reason therefore is conjectured as follows.
  • a shape, application and the like of the cutting tool of the present embodiment are not particularly limited as long as it is a cutting tool
  • the cutting tool of the present embodiment can be, for example, drills, end mills, replacement blade inserts for milling, replacement blade inserts for turning, metal saws, gear cutting tools, reamers, taps, inserts for pin milling of crankshafts, or the like.
  • FIG. 1 is a schematic partial cross-sectional view illustrating an example of the configuration of the cutting tool of the present embodiment.
  • a cutting tool 100 comprises a base material 10 and a coating 20 arranged on base material 10 .
  • Base material 10 is not particularly limited, Base material 10 can be configured of, for example, such as cemented carbide, cermet, high-speed steel, ceramics, a cubic boron nitride sintered material, and a diamond sintered material. Base material 10 is preferably made of cemented carbide, This is because the cemented carbide has excellent wear resistance.
  • Cemented carbide is a sintered material composed mainly of WC (tungsten carbide) particles.
  • the cemented carbide includes a hard phase and a binder phase.
  • the hard phase contains WC particles.
  • the binder phase bonds the WC particles to each other.
  • the binder phase contains, for example, Co (cobalt) and the like.
  • the binder phase may further contain, for example, TiC (titanium carbide), TaC (tantalum carbide), NC (niobium carbide), or the like.
  • the cemented carbide may contain impurities that are unavoidably mixed in during a manufacturing process.
  • the cemented carbide may also contain free carbon or an anomalous layer referred to as “ ⁇ -layer” in the microstructure.
  • the cemented carbide may undergo surface modification treatment.
  • the cemented carbide may contain a ⁇ -free layer or the like on a surface thereof.
  • the cemented carbide preferably contains 87% by mass or more and 96% by mass or less of WC particles and contains 4% by mass or more and 13% by mass or less of Co.
  • the WC particle preferably has an average particle size of 0.2 ⁇ m or larger and 4 ⁇ m or smaller.
  • Co is softer than the WC particle.
  • soft Co can be removed by ion bombardment treatment on a surface of base material 10 .
  • cemented carbide having the aforementioned composition and the WC particle having the aforementioned average particle size moderate convex and concave will be formed on a surface after Co was removed.
  • Coating 20 formed on such a surface is considered to exhibit an anchor effect, thereby improving adhesiveness between coating 20 and base material 10 .
  • the particle size of the WC particle indicates the diameter of a circle circumscribed by a two-dimensional projected image of the WC particle.
  • the particle size is determined with a scanning electron microscope (SEM) or a transmission electron microscope (TEM). Namely, cemented carbide is cut, and the cut surface is observed by SEM or TEM.
  • the diameter of the circle circumscribed to the WC particle in an observed image is regarded as the particle diameter of the WC particle.
  • the diameters of 10 or more (preferably 50 or more and more preferably 100 or more) of WC particles selected at random in the observed image are measured, and the arithmetic mean value thereof is considered to be an average particle diameter of the WC particles.
  • the cut surface is desirably subjected to cross-section processing by a cross-section polisher (CP) or focused ion beam (FIB) or the like.
  • CP cross-section polisher
  • FIB focused ion beam
  • Coating 20 is arranged on base material 10 .
  • Coating 20 may be arranged on a portion of a surface of base material 10 or on the entire surface thereof. However, coating 20 shall be arranged on at least a portion of the surface of base material 10 , which corresponds to a cutting edge.
  • the stacked configuration of coatings 20 is not necessarily uniform throughout the entire coating 20 , and may partially be different.
  • the thickness of coating 20 is preferably 1.0 ⁇ m or more and 25 ⁇ m or less. Coating 20 having a thickness of 1.0 pm or more improves the wear resistance. Coating 20 having a thickness of 25 ⁇ m or less improves the chipping resistance.
  • the thickness of coating 20 is preferably 1.0 ⁇ m or more and 25 ⁇ m or less, more preferably 2.0 ⁇ m or more and 16 ⁇ m or less, and still more preferably 3.0 ⁇ m or more and 12 ⁇ m or less.
  • the thickness of the coating refers to the total summation of each thickness of the layers constituting the coating. Examples of the “layer constituting the coating” include, for example, first layer, second layer, third layer, and the like.
  • each layer constituting the coating is determined by obtaining a thin sample thereinafter also referred to as “cross-sectional sample”) of a cross-section parallel to the normal direction of the surface of the base material of the cutting tool and observing the cross-sectional sample with a scanning transmission electron microscope (STEM).
  • STEM scanning transmission electron microscope
  • Examples of the scanning transmission electron microscope include, for example, a JEM-2100F (trade name) manufactured by JEOL Ltd.
  • Observation magnification of the cross-sectional sample is set at 5,000 to 10,000 times, thicknesses of each layer are measured at five locations thereof, and an arithmetic mean of the thicknesses is used as the “thickness of each layer.”
  • a first layer 21 has a multilayer structure in which first unit layer 1 and second unit layer 2 are alternately stacked, As long as first layer 21 includes one or more of first unit layers 1 and one or more of second unit layers 2 , respectively, the number of stacking is not limited. The number of stacking indicates the total number of first unit layer 1 and second unit layer 2 , included in first layer 21 . The number of stacking is preferably more than 10 and 5,000 or less, preferably 200 or more and 5,000 or less, more preferably 400 or more and 2,000 or less, and still more preferably 500 or more and 1,000 or less.
  • the layer closest to base material 10 may be first unit layer 1 or second unit layer 2 .
  • the layer farthest from base material 10 may be first unit layer 1 or second unit layer 2 .
  • the thickness of the first layer is 1.0 ⁇ m or more and 20 ⁇ m or less.
  • the first layer having a thickness of 1.0 ⁇ m or more improves the wear resistance.
  • the first layer having a thickness of 20 ⁇ m or less improves the chipping resistance.
  • the lower limit of the thickness of the first layer is preferably 1.0 ⁇ m or more, more preferably 2.0 ⁇ m or more, and still more preferably 3.0 ⁇ m or more.
  • the upper limit of the thickness of the first layer is preferably 20 ⁇ m or less, preferably 18 ⁇ m or less, more preferably 16 ⁇ m or less, and still more preferably 12 ⁇ m or less.
  • the thickness of the first layer is 1.0 ⁇ m or more and 20 ⁇ m or less, preferably 2.0 ⁇ m or more and 16 ⁇ m or less, and more preferably 3.0 ⁇ m or more and 12 ⁇ m or less.
  • First unit layer 1 and second unit layer 2 each have a thickness of 2 nm or more and less than 50 nm.
  • the alternate repetition of such thin layers can inhibit cracks from progressing.
  • First unit layer 1 and second unit layer 2 each having a thickness of less than 2 nm may lower the inhibition effect of crack propagation due to mixing of compositions of first unit layer 1 and second unit layer 2 .
  • first unit layer 1 and second unit layer 2 each having a thickness of 50 nm or more may lower the inhibition of interlayer delamination,
  • the lower limit of the thickness of the first unit layer is 2 nm or more, preferably 4 nm or more, more preferably 6 nm or more, and still more preferably 8 nm or more.
  • the upper limit of the thickness of the first unit layer is less than 50 nm, preferably 46 nm or less, preferably 40 nm or less, and more preferably 30 nm or less.
  • the thickness of the first unit layer is 2 nm or more and less than 50 nm, preferably 4 nm or more to 40 nm or less and more preferably 6 nm or more and 30 nm or less.
  • the lower limit of the thickness of the second unit layer is 2 nm or more, preferably 4 nm or more, more preferably 6 nm or more, and still more preferably 8 nm or more.
  • the upper limit of the thickness of the second unit layer is less than 50 nm, preferably 47 nm or less, more preferably 40 nm or less, and still more preferably 30 nm or less.
  • the thickness of the second unit layer is 2 nm or more and less than 50 nm, preferably 4 nm or more and 40 nm or less, and more preferably 6 nm or more and nm or less.
  • the thickness of the first unit layer is measured according to the procedure described above. An arithmetic mean value of the thicknesses of the five first unit layers is determined. The arithmetic mean value is taken as the thickness of the first unit layer.
  • the thickness of the second unit layer is measured according to the procedure described above. An arithmetic mean value of the thicknesses of the five second unit layers is determined. The arithmetic mean value is taken as the thickness of the second unit layer.
  • the first unit layer is composed of Ti a Al b B c N
  • compositions of first unit layer 1 and second unit layer 2 preferably satisfy the relationship 0.05 ⁇ a ⁇ d ⁇ 0.15 and 0.05 ⁇ e ⁇ b ⁇ 0.15 and more preferably 0.05 ⁇ a ⁇ d ⁇ 0.10 and 0.05 ⁇ e ⁇ b ⁇ 0.10. This further improves the inhibition effects of crack propagation and interlayer delamination.
  • the lower limit of “a” is 0.54 or more, preferably 0.57 or more and more preferably 0.60 or more,
  • the upper limit of “a” is 0.75 or less, preferably 0.72 or less, and, more preferably 0.69 or less.
  • “a” preferably satisfies 0.57 ⁇ a ⁇ 0.72 and more preferably 0.60 ⁇ a ⁇ 0.69.
  • the lower limit of “c” is more than 0, preferably 0.01 or more and more preferably 0.02 or more,
  • the upper limit of “c” is 0.10 or less, preferably 0.09 or less, and more preferably 0.08 or less.
  • “c” preferably satisfies 0.01 ⁇ c ⁇ 0.09 and more preferably 0.02 ⁇ c ⁇ 0.08.
  • the lower limit of “f” is more than 0, preferably 0.01 or more and more preferably 0.02 or more.
  • the upper limit of “f” is 0.10 or less, preferably 0.09 or less, and more preferably 0.08 or less. “f” preferably satisfies 0.01 ⁇ f ⁇ 0.09 and more preferably 0.02 ⁇ f ⁇ 0.08.
  • the subscripts of a b, c in Ti a Al b B c N of the first unit layer, and d, e, f in Ti d Al c B f N of the second unit layer were identified by measuring the composition of each layer by energy dispersive X-ray spectrometry (EDX).
  • EDX energy dispersive X-ray spectrometry
  • a TEM-EDX is used for composition analysis.
  • Examples of the EDX apparatus include a JED-2300 (trade name) manufactured by JEOL Ltd.
  • compositions of five layers of each of the first unit layer and the second unit layer are analyzed and the second unit layer, and an average composition of the first unit layer for the five layers and an average composition of the second unit layer for the five layers are determined, respectively.
  • the average composition of the first unit layer for the five layers is taken as a composition of the first unit layer; and the average composition of the second unit layer for the five layers is taken as a composition of the second unit layer. Based on these compositions, a, b, c, d, e, and fare identified.
  • the titanium content in the first layer is measured by TEM-EDX.
  • Examples of an EDX apparatus includes an apparatus such as a JED-2300 (trade name) manufactured by JEOL Ltd.
  • the titanium content in the first layer is measured by the following procedure.
  • the first layer is preferably composed of a plurality of crystal grains with the diameter of the largest inscribed circle of the crystal grain of 50 nm or smaller. According thereto, the first layer has a dense microstructure, thereby improving the wear resistance and chipping resistance of the cutting tool.
  • the first layer of the present disclosure may include a region that does not constitute a crystal grain (region where atoms are arranged at random) together with the plurality of crystal grains to the extent that the effect of the present disclosure is not impaired.
  • the diameter of the largest inscribed circle of the crystal grain is preferably 5 nm or greater and 50 nm or smaller, more preferably 7 nm or greater and 45 nm or smaller, and still more preferably 10 nm or greater and 40 nm or smaller.
  • a method for measuring the diameter of the largest inscribed circle of the above crystal grain is as follows.
  • a thin sample of a cross-section of the cutting tool parallel to the normal direction of a surface of the base material (thickness: approximately 10 to 100 nm, hereinafter also referred to as “cross-sectional sample”) is obtained.
  • the cross-sectional sample is then subjected to transmission electron microscopy (TEM) to obtain a bright field image.
  • TEM transmission electron microscopy
  • the observation magnification is set to 1 million to 5 million times. As shown in FIG.
  • the bright field image is acquired so as to include a region A sandwiched between a line L 2 at a distance of 0.2 ⁇ m from a line L 1 indicating the center of the first layer in the thickness direction, to the base material side, and a line L 3 at the distance of 0.2 ⁇ m from line L 1 to the side on a surface of the coating.
  • a rectangular measurement field of view of 150 nm ⁇ 150 nm is arbitrarily set within region A.
  • FIG. 3 is a schematic view illustrating an example of a bright field image of the above measurement field.
  • atoms are indicated by black dots with a symbol 50 . Note, however, in FIG. 3 , a portion of the atoms is shown.
  • the line segments are shown as L 10 to L 14 , L 20 to L 22 , and L 30 to L 34 .
  • a grain is defined as a region where the angle between each line segment is ⁇ 0.5° or less (i.e., ⁇ 0.5° or more and 0.5° or less).
  • each line segment L 10 to L 14 stay within ⁇ 0.5° or less, and the region including these line segments corresponds to a grain 24 a .
  • the angles between each line segment L 20 to L 22 stay within ⁇ 0.5° or less, and the region including these line segments corresponds to a grain 24 b .
  • the angles between each line segment L 30 to L 34 stay within ⁇ 0.5° or less and the region including these line segments corresponds to a grain 24 c.
  • the diameter of the largest inscribed circle 25 a of grain 24 a is D 1 .
  • the diameter of the largest inscribed circle 25 b of grain 24 b is D 2 .
  • the diameter of the largest inscribed circle 25 c of grain 24 c is D 3 .
  • D 1 , D 2 and D 3 are all 50 nm or smaller, it is confirmed that the first layer shown in FIG. 3 is composed of a plurality of crystal grains, and the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
  • Detector One dimensional semiconductor detector
  • Nanoindentation hardness H of the first layer at 25° C. is preferably 30 GPa or greater. Accordingly, the wear resistance of the cutting tool is improved.
  • the lower limit of nanoindentation hardness H is preferably 30 GPa or greater, more preferably 34 GPa or greater, and still more preferably 38 GPa or greater.
  • the upper limit of nanoindentation hardness H is not particularly limited, and can be set to 60 GPa or smaller from the viewpoint on manufacturing. Nanoindentation hardness H is preferably 30 GPa or greater and 60 GPa or smaller, and more preferably 34 GPa or greater and 60 GPa or smaller, and still more preferably 38 GPa or greater and 60 GPa or smaller.
  • Nanoindentation hardness H of the above first layer at 25° C. is calculated by a nanoindentation method complied with the standard procedure set forth in “ISO 14577-1:2015 Metallic materials-Instrumented indentation test for hardness and materials parameters.”
  • a measurement apparatus that is an “ENT-1100a” manufactured by Elionix Inc,, is used.
  • An indentation load of an indenter is 1 g, Indentation of the indenter is conducted along a cross-section of the first layer in the vertical direction (i.e., parallel to a surface of the base material) for the first layer exposed in the cross-section parallel to the normal direction of the surface of the base material.
  • the aforementioned measurement is conducted for five measurement samples, and an average value of the nanoindentation hardness obtained for each sample is taken as nanoindentation hardness of the first layer. Data that appear to be anomalous values at first glance shall be excluded.
  • a ratio of nanoindentation hardness H (GPa) of the first layer at 25° C. to Young's modulus E (GPa) of the first layer at 25° C., H/E, is preferably 0.070 or more. According thereto, the cutting tool can have excellent wear resistance as well as chipping resistance, thereby further improving the tool life. From the viewpoint of excellent balance between the wear resistance and chipping resistance, the H/E value is preferably 0.070 or more, more preferably 0.073 or more, and still more preferably 0.076 or more.
  • the upper limit of H/E is not particularly limited, and can be set to 0.120 or less from the viewpoint on manufacturing. H/E is preferably 0.070 or more and 0.120 or less, more preferably 0.073 or more and 0.120 or less, and still more preferably 0.076 or more and 0.120 or less.
  • the aforementioned nanoindentation hardness H is preferably 30 GPa or greater and 50 GPa or smaller, more preferably 35 GPa or greater and 50 GPa or smaller, and still more preferably 40 GPa or greater and 50 GPa or smaller.
  • Young's modulus E is preferably 350 GPa or greater and 600 GPa or smaller, more preferably 350 GPa or greater and 550 GPa or smaller, and still more preferably 350 GPa or greater and 500 GPa or smaller. Young's modulus E is measured by the same method and under the same conditions as nanoindentation hardness H described above.
  • Embodiment 2 a method for manufacturing the cutting tool of Embodiment 1 will be described.
  • the manufacturing method can include a step of preparing a base material and a step of forming a coating on the base material. Details of each step will be described below.
  • Base material 10 that is the base material described in Embodiment 1 can be used.
  • an arc discharge is generated with a target material as a cathode. This evaporates and ionizes the target material. Ions are then deposited on a surface of base material 10 to which a negative bias voltage is applied.
  • the AIP method is superior in ionization rate of the target material.
  • a deposition apparatus 200 is equipped with a chamber 201 .
  • Chamber 201 has a gas inlet port 202 for introducing a raw material gas to chamber 201 and a gas exhaust port 203 for discharging the material gas from inside chamber 201 to an outside.
  • Gas exhaust port 203 is connected to a vacuum pump, which is not shown in the figure. Pressure in chamber 201 is adjusted by the amount of gas introduced and discharged.
  • a rotary table 204 is disposed in chamber 201 .
  • a base material holder 205 for holding base material 10 is attached to rotary table 204 .
  • Base material holder 205 is connected to a negative electrode of a bias power supply 206 .
  • a positive electrode of bias power supply 206 is grounded.
  • a plurality of target materials 211 , 212 , 213 , 214 is attached to side walls of chamber 201 , As shown in Fig, 3 , each of target materials 211 and 212 is connected to negative electrodes of direct current power supplies 221 and 222 . Direct current power supplies 221 and 222 are variable power supplies, and their positive electrodes are grounded. The same is true for target materials 213 and 214 , although not shown in FIG. 3 . Specific operations will be described below.
  • a base material holder 205 holds base material 10 .
  • chamber 201 is adjusted to the inside pressure of 1.0 ⁇ 10 ⁇ 4 Pa.
  • base material 10 is adjusted to a temperature of 500° C. by a heater (not shown) attached to deposition apparatus 200 .
  • a coating in the case of including second layer 22 forms second layer 22 on a surface of base material 10 .
  • a TiCN layer, TiN layer, or TiCNO layer is formed on the surface of base material 10 .
  • first layer 21 is formed on the surface of base material 10 or on a surface of second layer 22 .
  • a sintered alloy containing Ti, Al and B is used as a target material.
  • Each target material is set at a predetermined position, nitrogen gas is introduced from gas inlet port 202 to form first layer 21 while rotating rotary table 204 .
  • Forming conditions of first layer 21 are as follows.
  • Bias voltage ⁇ 400 to ⁇ 30 V
  • the base material temperature, reaction gas pressure, bias voltage, and arc current are set to constant values within the ranges described above, or varied continuously within the above ranges.
  • the first unit layer and second unit layer can be appropriately formed in combinations of the methods (A) to (D) below.
  • a gas flow rate is varied.
  • the gas flow rate upon forming of the first unit layer can be set to 500 sccm to 2000 sccm
  • the gas flow rate upon forming of the second unit layer can be set to 500 sccm to 2000 sccm.
  • base material 10 is rotated to control a rotation cycle.
  • the rotation cycle can be set to 1 rpm to 5 rpm.
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer
  • a nanoindentation hardness H of the first layer at 25° C. is 30 GPa or greater.
  • a ratio of a nanoindentation hardness H of the first layer at 25° C. to a Young's modulus E of the first layer at 25° C., H/E, is 0.070 or more.
  • the thickness of the coating is preferably 1.0 ⁇ m or more and 25 ⁇ m or less.
  • the thickness of the coating is preferably 2.0 pm or more and 16 pm or less.
  • the total number of stacking of the first unit layer and the second unit layer included in the first is preferably more than 10 and 5000 or less.
  • the above number of stacking is preferably 200 or more and 5000 or less.
  • the above number of stacking is preferably 400 or more and 2000 or less.
  • the above number of stacking is preferably 500 or more and 1000 or less.
  • the thickness of the first layer is preferably 2.0 ⁇ m or more and 16 ⁇ m or less.
  • the thickness of the first layer is preferably 3.0 ⁇ m or more and 12 ⁇ m or less.
  • a cutting tool is fabricated as follows and a tool life was evaluated.
  • a cutting insert made of cemented carbide (model number: SEMT13T3AGSR manufactured by Sumitomo Electric Hardmetal Ltd.) was prepared as a base material.
  • the cemented carbide contains WC particles (90% by mass) and Co (10% by mass) The average particle size of the WC particle is 2 ⁇ m.
  • a coating was formed on the aforementioned base material by using a deposition apparatus having the configuration shown in FIGS. 4 and 5 .
  • a surface of the base material was cleaned by ion bombardment treatment with Ar ions.
  • the specific conditions of the ion bombardment treatment are as described in Embodiment 2.
  • the target materials were set at predetermined positions in the deposition apparatus. Nitrogen gas was introduced from the gas inlet port, and the first layer was formed while rotating the rotary table.
  • the first layer forming conditions base material temperature, bias voltage, arc current, and reaction gas pressure
  • a rotation speed of the rotary table was adjusted according to the film thicknesses of the first unit layer and second unit layer.
  • a cutting test was carried out by using the cutting tool of each sample under the following conditions, and a cutting time (minutes) until the width of crater wear reached 0.3 mm or more was measured. The cutting time longer than 24 minutes is determined that the cutting tool has excellent wear resistance. The results are shown in the “Cutting test 1” column of Tables 5 and 6.
  • the above cutting conditions correspond to those for stainless steel milling (low-speed, high-feed machining).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Drilling Tools (AREA)
  • Cutting Tools, Boring Holders, And Turrets (AREA)

Abstract

A cutting tool comprising a base material and a coating, wherein the coating includes a first layer having a multilayer structure in which a first unit layer and a second unit layer; a thickness of the first unit layer is 2 nm or more and less than 50 nm; a thickness of the second unit layer is 2 nm or more and less than 50 nm; a thickness of the first layer is 1.0 μm or more and 20 μm or less, the first unit layer is TiaAlbBcN, and the second unit layer is TidAleBfN, wherein 0.54≤a≤0.75, 0.24≤b≤0.45, 0<c≤0.10, a+b+c=1.00, 0.44≤d≤0.65, -.34≤e≤0.55, 0<f≤0.10, d+e+f=1.00, 0.05≤a−d≤0.20, and 0.05≤e−b≤0.20 are satisfied, and a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.

Description

    TECHNICAL FIELD
  • The present disclosure relates to a cutting tool.
  • BACKGROUND ART
  • Conventionally, coatings that coat a surface of a base material made of cemented carbide, sintered cubic boron nitride and the like have been developed in order to improve performance of cutting tools (for example, Patent Literature 1 and Patent Literature 2).
  • CITATION LIST Patent Literature
  • PTL 1: Japanese Patent Laying-Open No. 2017-193004
  • PTL 2: Japanese Patent Laying-Open No. 2011-224717
  • SUMMARY OF INVENTION
  • The cutting tool of the present disclosure is a cutting tool comprising a base material and a coating arranged on the base material, wherein
      • the coating includes a first layer;
      • the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
      • a thickness of the first unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the second unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the first layer is 1.0 um or more and 20 μm or less,
      • the first unit layer is composed of TiaAlbBcN, and
      • the second unit layer is composed of Ti3AleBfN,
  • wherein

  • 0.54≤a≤0.75,

  • 0.24≤b≤0.45,

  • 0<c≤0.10,

  • a+b+c=1.00,

  • 0.44≤d≤0.65,

  • 0.34≤e≤0.55,

  • 0<f≤0.10,

  • d+3+f=1.00,

  • 0.05≤a−d≤0.20, and

  • 0.05≤e−b≤0.20 are satisfied, and
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum arid boron is 50% or more in the first layer.
  • BRIEF DESCRIPTION OF DRAWINGS
  • FIG. 1 is a schematic cross-sectional view illustrating an example of the configuration of the cutting tool according to one embodiment of the present disclosure.
  • FIG. 2 is a view explaining a measurement region when measuring the diameter of the largest inscribed circle of a crystal grain of a first layer.
  • FIG. 3 is a schematic view explaining a method for measuring the diameter of the largest inscribed circle of a crystal grain of a first layer, a schematic view illustrating a bright field image of a measurement field of view.
  • FIG. 3A is a view explaining positional relationship between a crystal grain, a first unit layer and a second unit layer.
  • FIG. 4 is a schematic cross-sectional view illustrating an example of the configuration of a film deposition apparatus.
  • FIG. 5 is a schematic cross-sectional view illustrating an example of the configuration of a film deposition apparatus.
  • DETAILED DESCRIPTION Problem to be Solved by the Present Disclosure
  • In recent years, cost reduction of tools has been increasingly demanded, and the tools have been required for their longer lives. For example, in the machining of stainless steel, cutting tools with their long tool lives are required in terms of both high-speed, low-feed machining and low-speed, high-feed machining.
  • Then, an object of the present disclosure is to provide a cutting tool with a long tool life.
  • ADVANTAGEOUS EFFECTS OF THE PRESENT DISCLOSURE
  • The cutting tool of the present disclosure can have a long tool life.
  • Description of Embodiments
  • First, aspects of the present disclosure will be described by listing them.
  • (1) The cutting tool of the present disclosure is a cutting tool comprising a base material and a coating arranged on the base material, wherein
  • the coating includes a first layer;
  • the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
      • a thickness of the first unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the second unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the first layer is 1.0 μm or more and 20 μm or less,
      • the first unit layer is composed of TiaAlbBcN, and
      • the second unit layer is composed of TidAleBfN,
  • wherein

  • 0.54≤a≤0.75

  • 0.24≤b≤0.45,

  • 0<c≤0.10,

  • a+b+c=1.00,

  • 0.44≤d≤0.65,

  • 0.34≤e≤0.55,

  • 0<f≤0.10,

  • d+e+f=1.00,

  • 0.05≤a−d≤0.20, and

  • 0.05≤e−b≤0.20 are satisfied, and
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.
  • The cutting tool of the present disclosure can have a long tool life.
  • (2) The first layer is composed of a plurality of crystal grains and
  • the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
  • Accordingly, the microstructure of the first layer is dense, thereby improving wear resistance and chipping resistance of the cutting tool.
  • (3) In an X-ray diffraction spectrum of the first layer, a half width of a diffraction peak derived from (200) plane of a cubic crystal is preferably 0.2° or more and 2.0° or less.
  • Accordingly, the proportion of the cubic crystal structure in the first layer is high, thereby enabling high hardness of the first layer, which results in improvements in the wear resistance of the cutting tool.
  • (4) Nanoindentation hardness H of the first layer at 25° C. is preferably 30 GPa
  • or greater. Accordingly, the wear resistance of the cutting tool is improved.
  • (5) A ratio of a nanoindentation hardness H (GPa) of the first layer at 25° C. to a Young's modulus E (GPa) of the first layer at 25° C., HIE, is preferably 0.07 or more.
  • Accordingly, the cutting tool can have excellent wear resistance as well as chipping resistance, enabling further improvements in its tool life.
  • Details of Embodiments of the Present Disclosure
  • Specific examples of the cutting tool of the present disclosure will be described with reference to the drawings below. In the drawings of the present disclosure, the same reference sign represents the same portion or equivalent portion. Moreover, dimensional relationships such as length, width, thickness, and depth have been changed as necessary for the sake of clarity and simplification of the drawings, and do not necessarily represent actual dimensional relationships.
  • In the present disclosure, the notation in the form “A to B” refers to the upper limit and lower limit of the range (i.e., A or more and B or less). In a case in which no units are described in A, but only in B, the units in A are the same as that in B.
  • Compounds and the like when represented by chemical formulae in the present disclosure shall include all conventionally known atomic ratios as long as the atomic ratios thereof and not particularly limited, and should not necessarily be limited only to those in their stoichiometric ranges. For example, when described as “TiN”, the ratio of the number of atoms constituting TiN includes all conventionally known atomic ratios.
  • In the present disclosure, when each of one or more numerical values is described as lower limits and upper limits of a numerical range, combinations of any one numerical value described for the lower limit and any one numerical value described for the upper limit shall also be disclosed. For example, when a1 or more, b1 or more, or c1 or more is described as the lower limit, and a2 or less, b2 or less, and c2 or less as the upper limit, a1 or more and a2 or less, a1 or more and b2 or less, a1 or more and c2 or less, and b1 or more and a2 or less, b1 or more and to b2 or less, b1 or more and c2 or less, c1 or more and a2 or less, and c1 or more and b2 or less, and c1 or more and c2 or less, shall be disclosed.
  • Embodiment 1: Cutting Tool
  • One embodiment of the cutting tool of the present disclosure (hereinafter also referred to as “present embodiment”) is a cutting tool comprising a base material and a coating arranged on the base material, wherein
      • the coating includes a first layer;
      • the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
      • a thickness of the first unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the second unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the first layer is 1.0 μm or more and 20 μm or less,
      • the first unit layer is composed of TiaAlbBcN, and
      • the second unit layer is composed of TidAleBfN,
  • wherein

  • 0.54≤a≤0.75,

  • 0.24≤b≤0.45,

  • 0<c≤0.10,

  • a+b+c=1.00

  • 0.44≤d≤0.65,

  • 0.34≤e≤0.55,

  • 0<f≤0.10,

  • d+e+f=1.00,

  • 0.055≤a−d≤0.20, and

  • 0.05e−b≤0.20 are satisfied, and
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.
  • The cutting tool of the present disclosure can have a long tool life. The reason therefore is conjectured as follows.
      • (i) The coating of the cutting tool of the present disclosure includes a first layer having a multilayer structure in which the first unit layer and the second unit layer are alternately stacked. The composition of the first unit layer and that of the second unit layer are different from each other, This enables to inhibit propagation of cracks occurring from a surface of the coating in the vicinity of an interface between the first unit layer and the second unit layer upon using the cutting tool. Moreover, the thickness of each of the first unit layer and the second unit layer, which is very small and 2 nm or more and less than 50 nm, allows the first layer and second layer in a large number to be stacked, thereby further enhancing inhibition effect of crack propagation. Therefore, large scale damage to the coating can be inhibited, thereby prolonging a tool life of the cutting tool.
      • (ii) In the first layer described above, the composition of the first unit layer and that of the second unit layer are different enough to inhibit crack propagation as described in (i) above as well as are similar to the extent that allows the crystal lattice to be continuous, as a result of which the first unit layer and the second unit layer are inhibited for delaminating therebetween, thereby prolonging a tool life of the cutting tool,
      • (iii) In the above first layer, a percentage of the number of atoms of titanium (Ti) to the total number of atoms of titanium, aluminum and boron (Ti+Al+B). which is {Ti/(Ti−Al+B)}×100, is 50% or more. According thereto, the first layer can have excellent the wear resistance and chipping resistance. Furthermore, in the above first layer, a percentage of the number of atoms of boron (B) to the total number of atoms of titanium, aluminum and boron (Ti+Al+B), which is {B/(Ti+Al+B)}×100, is 10% or less. According thereto, the crystal grains constituting the first layer micronize, further improving the wear resistance and chipping resistance. Therefore, the tool life of the cutting tool is prolonged.
    <Cutting Tool>
  • A shape, application and the like of the cutting tool of the present embodiment are not particularly limited as long as it is a cutting tool, The cutting tool of the present embodiment can be, for example, drills, end mills, replacement blade inserts for milling, replacement blade inserts for turning, metal saws, gear cutting tools, reamers, taps, inserts for pin milling of crankshafts, or the like.
  • FIG. 1 is a schematic partial cross-sectional view illustrating an example of the configuration of the cutting tool of the present embodiment. A cutting tool 100 comprises a base material 10 and a coating 20 arranged on base material 10.
  • <<Base Material>>
  • Base material 10 is not particularly limited, Base material 10 can be configured of, for example, such as cemented carbide, cermet, high-speed steel, ceramics, a cubic boron nitride sintered material, and a diamond sintered material. Base material 10 is preferably made of cemented carbide, This is because the cemented carbide has excellent wear resistance.
  • Cemented carbide is a sintered material composed mainly of WC (tungsten carbide) particles. The cemented carbide includes a hard phase and a binder phase. The hard phase contains WC particles. The binder phase bonds the WC particles to each other. The binder phase contains, for example, Co (cobalt) and the like. The binder phase may further contain, for example, TiC (titanium carbide), TaC (tantalum carbide), NC (niobium carbide), or the like.
  • The cemented carbide may contain impurities that are unavoidably mixed in during a manufacturing process. The cemented carbide may also contain free carbon or an anomalous layer referred to as “η-layer” in the microstructure. Furthermore, the cemented carbide may undergo surface modification treatment. For example, the cemented carbide may contain a β-free layer or the like on a surface thereof.
  • The cemented carbide preferably contains 87% by mass or more and 96% by mass or less of WC particles and contains 4% by mass or more and 13% by mass or less of Co. The WC particle preferably has an average particle size of 0.2 μm or larger and 4 μm or smaller.
  • Co is softer than the WC particle. As will be described below, soft Co can be removed by ion bombardment treatment on a surface of base material 10. With cemented carbide having the aforementioned composition and the WC particle having the aforementioned average particle size, moderate convex and concave will be formed on a surface after Co was removed. Coating 20 formed on such a surface is considered to exhibit an anchor effect, thereby improving adhesiveness between coating 20 and base material 10.
  • Here, the particle size of the WC particle indicates the diameter of a circle circumscribed by a two-dimensional projected image of the WC particle. The particle size is determined with a scanning electron microscope (SEM) or a transmission electron microscope (TEM). Namely, cemented carbide is cut, and the cut surface is observed by SEM or TEM. The diameter of the circle circumscribed to the WC particle in an observed image is regarded as the particle diameter of the WC particle. In the observed image, the diameters of 10 or more (preferably 50 or more and more preferably 100 or more) of WC particles selected at random in the observed image are measured, and the arithmetic mean value thereof is considered to be an average particle diameter of the WC particles. Upon the observation, the cut surface is desirably subjected to cross-section processing by a cross-section polisher (CP) or focused ion beam (FIB) or the like.
  • <<Coating>>
  • Coating 20 is arranged on base material 10. Coating 20 may be arranged on a portion of a surface of base material 10 or on the entire surface thereof. However, coating 20 shall be arranged on at least a portion of the surface of base material 10, which corresponds to a cutting edge.
  • Coating 20 includes a first layer 21. Coating 20 may include other layers as long as it includes first layer 21. For example, coating 20 may include a second layer 22 arranged between base material 10 and first layer 21 and/or a third layer 23 arranged on the top surface of coating 20. A publicly known underlying layer can be applied to the second layer. Examples of the underlying layer include a TiCN layer, a TiN layer, a TiCNO layer, or the like. A publicly known surface layer can be applied to the third layer. The surface layers include a TiC layer, TiN layer, TiCN layer, or the like.
  • The stacked configuration of coatings 20 is not necessarily uniform throughout the entire coating 20, and may partially be different.
  • The thickness of coating 20 is preferably 1.0 μm or more and 25 μm or less. Coating 20 having a thickness of 1.0 pm or more improves the wear resistance. Coating 20 having a thickness of 25 μm or less improves the chipping resistance. The thickness of coating 20 is preferably 1.0 μm or more and 25 μm or less, more preferably 2.0 μm or more and 16 μm or less, and still more preferably 3.0 μm or more and 12 μm or less. Here, the thickness of the coating refers to the total summation of each thickness of the layers constituting the coating. Examples of the “layer constituting the coating” include, for example, first layer, second layer, third layer, and the like.
  • The thickness of each layer constituting the coating is determined by obtaining a thin sample thereinafter also referred to as “cross-sectional sample”) of a cross-section parallel to the normal direction of the surface of the base material of the cutting tool and observing the cross-sectional sample with a scanning transmission electron microscope (STEM). Examples of the scanning transmission electron microscope include, for example, a JEM-2100F (trade name) manufactured by JEOL Ltd. Observation magnification of the cross-sectional sample is set at 5,000 to 10,000 times, thicknesses of each layer are measured at five locations thereof, and an arithmetic mean of the thicknesses is used as the “thickness of each layer.”
  • It has been confirmed that as long as the same cutting tool is used for measurement, there is no variation in measurement results even though a measurement location is arbitrarily selected.
  • In the present embodiment, a crystal grain constituting coating 20 is preferably a cubic crystal. The cubic crystal increases hardness and prolongs a tool life.
  • <<First Layer>>
  • A first layer 21 has a multilayer structure in which first unit layer 1 and second unit layer 2 are alternately stacked, As long as first layer 21 includes one or more of first unit layers 1 and one or more of second unit layers 2, respectively, the number of stacking is not limited. The number of stacking indicates the total number of first unit layer 1 and second unit layer 2, included in first layer 21. The number of stacking is preferably more than 10 and 5,000 or less, preferably 200 or more and 5,000 or less, more preferably 400 or more and 2,000 or less, and still more preferably 500 or more and 1,000 or less. In first layer 21, the layer closest to base material 10 may be first unit layer 1 or second unit layer 2. Moreover, in first layer 21, the layer farthest from base material 10 may be first unit layer 1 or second unit layer 2.
  • The thickness of the first layer is 1.0 μm or more and 20 μm or less. The first layer having a thickness of 1.0 μm or more improves the wear resistance. The first layer having a thickness of 20 μm or less improves the chipping resistance. The lower limit of the thickness of the first layer is preferably 1.0 μm or more, more preferably 2.0 μm or more, and still more preferably 3.0 μm or more. The upper limit of the thickness of the first layer is preferably 20 μm or less, preferably 18 μm or less, more preferably 16 μm or less, and still more preferably 12 μm or less. The thickness of the first layer is 1.0 μm or more and 20 μm or less, preferably 2.0 μm or more and 16 μm or less, and more preferably 3.0 μm or more and 12 μm or less.
  • <<Thicknesses of First Unit Layer and Second Unit Layer>>
  • First unit layer 1 and second unit layer 2 each have a thickness of 2 nm or more and less than 50 nm. The alternate repetition of such thin layers can inhibit cracks from progressing. First unit layer 1 and second unit layer 2 each having a thickness of less than 2 nm may lower the inhibition effect of crack propagation due to mixing of compositions of first unit layer 1 and second unit layer 2. Further, first unit layer 1 and second unit layer 2 each having a thickness of 50 nm or more may lower the inhibition of interlayer delamination,
  • The lower limit of the thickness of the first unit layer is 2 nm or more, preferably 4 nm or more, more preferably 6 nm or more, and still more preferably 8 nm or more. The upper limit of the thickness of the first unit layer is less than 50 nm, preferably 46 nm or less, preferably 40 nm or less, and more preferably 30 nm or less. The thickness of the first unit layer is 2 nm or more and less than 50 nm, preferably 4 nm or more to 40 nm or less and more preferably 6 nm or more and 30 nm or less.
  • The lower limit of the thickness of the second unit layer is 2 nm or more, preferably 4 nm or more, more preferably 6 nm or more, and still more preferably 8 nm or more. The upper limit of the thickness of the second unit layer is less than 50 nm, preferably 47 nm or less, more preferably 40 nm or less, and still more preferably 30 nm or less. The thickness of the second unit layer is 2 nm or more and less than 50 nm, preferably 4 nm or more and 40 nm or less, and more preferably 6 nm or more and nm or less.
  • The respective thicknesses of the first unit layer and the second unit layer are measured as follows. A thin sample (hereinafter also referred to as “cross-sectional sample”) of a cross-sectional section of the cutting tool parallel to the normal direction of a surface of the base material is obtained. Then the cross-sectional sample is observed with a scanning transmission electron microscope (STEM). Examples of the scanning transmission electron microscope include, for example, a JEM-2100F (trade name) manufactured by JEOL Ltd. Observation magnification of the cross-sectional sample shall be adjusted according to the thicknesses of first unit layer 1 and second unit layer 2. For example, the observation magnification can be approximately 1 million times. In one first unit layer, thicknesses are measured at five locations thereof. An arithmetic mean value of the thicknesses of the five locations in the first unit layer is calculated to determine the thickness of the first unit layer that is the arithmetic mean value. In one second unit layer, thicknesses are measured at five locations thereof.
  • For each of the five different first unit layers, the thickness of the first unit layer is measured according to the procedure described above. An arithmetic mean value of the thicknesses of the five first unit layers is determined. The arithmetic mean value is taken as the thickness of the first unit layer. For each of the five different second unit layers, the thickness of the second unit layer is measured according to the procedure described above. An arithmetic mean value of the thicknesses of the five second unit layers is determined. The arithmetic mean value is taken as the thickness of the second unit layer.
  • It has been confirmed that there is no variation in the measurement results even. though the measurement location is arbitrarily selected, as long as measuring with the same cutting tool.
  • <<Compositions of First Unit Layer and Second Unit Layer>>
  • The first unit layer is composed of TiaAlbBcN, and the second unit layer is composed of TidAleBfN, wherein 0.54≤a≤0.75, 0.24≤b≤0.45, 0<c≤0.10, a+b+c=1.00, 0.44≤d≤0.65, 0.34≤e≤0.55, 0<f≤0.10, d+e+f=1.00, 0.05≤a−d≤0.20, and 0.0525≤e−b≤0.20, are satisfied.
  • The compositions of the first unit layer and the second unit layer that satisfy 0.05≤a−d and 0.05≤e−b, allow the compositions of the first unit layer and the second unit layer to be diverged to the extent that cracks between first unit layer 1 and second unit layer 2 can be inhibited from propagating. At the same time, satisfying a−d≤0.20 and e−b≤0.20 allows the compositions of the first unit layer and the second unit layer to be approximated to the extent that interlayer delamination between first unit layer 1 and second unit layer 2 can be inhibited. The compositions of first unit layer 1 and second unit layer 2 preferably satisfy the relationship 0.05≤a−d≤0.15 and 0.05≤e−b≤0.15 and more preferably 0.05≤a−d≤0.10 and 0.05≤e−b≤0.10. This further improves the inhibition effects of crack propagation and interlayer delamination.
  • In the first unit layer, the lower limit of “a” is 0.54 or more, preferably 0.57 or more and more preferably 0.60 or more, The upper limit of “a” is 0.75 or less, preferably 0.72 or less, and, more preferably 0.69 or less. “a” preferably satisfies 0.57≤a≤0.72 and more preferably 0.60≤a≤0.69.
  • In the first unit layer, the lower limit of “b” is 0.24 or more, preferably 0.27 or more, and more preferably 0.30 or more. The upper limit of “b” is 0.45 or less, preferably 0.42 or less, and more preferably 0.39 or less. “b” preferably satisfies 0.27≤b≤0.42 and more preferably 0.30≤b≤0.39.
  • In the second unit layer, the lower limit of “d” is 0.44 or more, preferably 0.47 or more, and more preferably 0.50 or more. The upper limit of “d” is 0.65 or less, preferably 0.62 or less, and more preferably 0.59 or less. “d” preferably satisfies 0.47≤d≤0.62 and more preferably 0.50≤d≤0.59.
  • In the second unit layer, the lower limit of “e” is 0.34 or more, preferably 0.37 or more, and more preferably 0.40 or more. The upper limit of “e” is 0.55 or less, preferably 0.52 or less, and more preferably 0.49 or less. “e” preferably satisfies 0.37≤e≤0.52 and more preferably 0.40≤e≤0.49.
  • Where 0<c5_0.10 is satisfied in the first unit layer and O<E:0.10 is satisfied in the second unit layer, the crystal grains constituting the first layer micronize, thereby further improving wear resistance and chipping resistance.
  • In the first unit layer, the lower limit of “c” is more than 0, preferably 0.01 or more and more preferably 0.02 or more, The upper limit of “c” is 0.10 or less, preferably 0.09 or less, and more preferably 0.08 or less. “c” preferably satisfies 0.01≤c≤0.09 and more preferably 0.02≤c≤0.08.
  • In the second unit layer, the lower limit of “f” is more than 0, preferably 0.01 or more and more preferably 0.02 or more. The upper limit of “f” is 0.10 or less, preferably 0.09 or less, and more preferably 0.08 or less. “f” preferably satisfies 0.01≤f≤0.09 and more preferably 0.02≤f≤0.08.
  • The subscripts of a b, c in TiaAlbBcN of the first unit layer, and d, e, f in TidAlcBfN of the second unit layer were identified by measuring the composition of each layer by energy dispersive X-ray spectrometry (EDX). A TEM-EDX is used for composition analysis. Examples of the EDX apparatus include a JED-2300 (trade name) manufactured by JEOL Ltd.
  • The above composition analysis is conducted by the following procedure. A thin sample (hereinafter referred to as “cross-sectional sample”) of a cross-section parallel to the normal direction of a surface of the base material of the cutting tool is obtained. While observing the cross-sectional sample with TEM, EDX analysis is conducted at five points arbitrarily selected within one first unit layer 1 or one second unit layer 2. The first unit layer and the second unit layer are distinguishable due to difference in contrast. Here, the “five points arbitrarily selected” shall be selected from grains that differ from each other. The composition of each of the first unit layer and the second unit layer is identified by arithmetically averaging composition ratios of each element, obtained from. the five measurements.
  • Compositions of five layers of each of the first unit layer and the second unit layer are analyzed and the second unit layer, and an average composition of the first unit layer for the five layers and an average composition of the second unit layer for the five layers are determined, respectively. The average composition of the first unit layer for the five layers is taken as a composition of the first unit layer; and the average composition of the second unit layer for the five layers is taken as a composition of the second unit layer. Based on these compositions, a, b, c, d, e, and fare identified.
  • As long as the measurement is carried out on the same cutting tool, it has been confirmed that there is no variation in the measurement results even though measurement points are arbitrarily selected.
  • <<Composition of First Layer>>
  • In the first layer, the percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron (hereinafter also referred to as “titanium content in the first layer”) is 50% or more. Accordingly, the first layer can have excellent wear resistance and chipping resistance. The lower limit of the titanium content in the first layer is 50% or more from the viewpoint of improving the wear resistance and chipping resistance, preferably 53% or more, and more preferably 56% or more. The upper limit of the titanium content in the first layer is preferably 72% or less and more preferably 69% or less from the viewpoint of improving heat resistance. The titanium content in the first layer is preferably 50% or more and 72% or less, more preferably 53% or more and 72% or less, and still more preferably 56% or more and 69% or less.
  • The titanium content in the first layer is measured by TEM-EDX. Examples of an EDX apparatus includes an apparatus such as a JED-2300 (trade name) manufactured by JEOL Ltd. The titanium content in the first layer is measured by the following procedure.
  • A thin sample (hereinafter also referred to as “cross-sectional sample”) of a cross-section parallel to the normal direction of a surface of the base material of the cutting tool is obtained. While observing the cross-sectional sample by TEM, EDX analysis is carried out at five fields of view arbitrarily selected within the first layer. Here, “five fields of view arbitrarily selected” are set so as not to overlap with each other. The range of one field of view is 200×200 nm. The arithmetic mean of the titanium content values obtained from the measurements of the five fields of view is taken as the titanium content of the first layer.
  • As long as the measurement is carried out on the same cutting tool, it has been confirmed that there is no variation in the measurement results even though measurement points are arbitrarily selected.
  • <<Diameter of Largest Inscribed Circle of Crystal Grains of First Layer>>
  • The first layer is preferably composed of a plurality of crystal grains with the diameter of the largest inscribed circle of the crystal grain of 50 nm or smaller. According thereto, the first layer has a dense microstructure, thereby improving the wear resistance and chipping resistance of the cutting tool. The first layer of the present disclosure may include a region that does not constitute a crystal grain (region where atoms are arranged at random) together with the plurality of crystal grains to the extent that the effect of the present disclosure is not impaired.
  • The upper limit of the diameter of the largest inscribed circle of the above crystal grain is preferably 50 nm or smaller from the viewpoint of improving the wear resistance and chipping resistance, more preferably 45 nm or smaller, and still more preferably 40 nm or smaller. The lower limit of the diameter of the largest inscribed circle of the crystal grain is preferably 5 nm or greater, more preferably 7 nm or greater, and still more preferably 10 nm or greater from the viewpoint of inhibiting a decrease in film hardness due to excessive micronization of crystal grains. The diameter of the largest inscribed circle of the crystal grain is preferably 5 nm or greater and 50 nm or smaller, more preferably 7 nm or greater and 45 nm or smaller, and still more preferably 10 nm or greater and 40 nm or smaller.
  • A method for measuring the diameter of the largest inscribed circle of the above crystal grain is as follows. A thin sample of a cross-section of the cutting tool parallel to the normal direction of a surface of the base material (thickness: approximately 10 to 100 nm, hereinafter also referred to as “cross-sectional sample”) is obtained. The cross-sectional sample is then subjected to transmission electron microscopy (TEM) to obtain a bright field image. The observation magnification is set to 1 million to 5 million times. As shown in FIG. 2 , the bright field image is acquired so as to include a region A sandwiched between a line L2 at a distance of 0.2 μm from a line L1 indicating the center of the first layer in the thickness direction, to the base material side, and a line L3 at the distance of 0.2 μm from line L1 to the side on a surface of the coating. A rectangular measurement field of view of 150 nm×150 nm is arbitrarily set within region A.
  • In the above measurement field of view, a region with atomic arrangement within ±0.5° or less is identified, and the region is defined as a crystal grain. In FIG. 3 , a method for identifying the area with atomic arrangement within ±0.5° or less and the crystal grain will be described.
  • FIG. 3 is a schematic view illustrating an example of a bright field image of the above measurement field. In FIG. 3 , atoms are indicated by black dots with a symbol 50. Note, however, in FIG. 3 , a portion of the atoms is shown. In the bright field image, atoms 50 regularly arranged are connected by a line segment such that the distance between atoms is closest. In FIG. 3 , the line segments are shown as L10 to L14, L20 to L22, and L30 to L34. A grain is defined as a region where the angle between each line segment is ±0.5° or less (i.e., −0.5° or more and 0.5° or less).
  • In FIG. 3 , the angles between each line segment L10 to L14 stay within ±0.5° or less, and the region including these line segments corresponds to a grain 24 a. The angles between each line segment L20 to L22 stay within ±0.5° or less, and the region including these line segments corresponds to a grain 24 b. The angles between each line segment L30 to L34 stay within ±0.5° or less and the region including these line segments corresponds to a grain 24 c.
  • The diameter of the largest inscribed circle of each grain in the above measurement field of view will be determined. The diameter of the largest inscribed. circle refers to the diameter of the largest inscribed circle that can be drawn inside the grain and contacts at least a portion of the outer edge of the grain.
  • In FIG. 3 , the diameter of the largest inscribed circle 25 a of grain 24 a is D1. The diameter of the largest inscribed circle 25 b of grain 24 b is D2. The diameter of the largest inscribed circle 25 c of grain 24 c is D3. Where D1, D2 and D3 are all 50 nm or smaller, it is confirmed that the first layer shown in FIG. 3 is composed of a plurality of crystal grains, and the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
  • It has been confirmed that there is no variation in the measurement results of the diameter of the largest inscribed circle of the crystal grain even though the above measurement field of view is arbitrarily set as long as the same cutting tool is used for the measurement.
  • In FIG. 3 , space is present between grain 24a, grain 24 b, and grain 24 c, however, crystal grains are actually present in the space. Since the thickness of a cross-sectional sample for TEM is approximately 10 to 100 nm, the bright field image also reflects information in the depth direction. In the region where plural crystal grains are overlapped in the thickness direction of the sample, regular atomic arrangement cannot be confirmed in the bright field image, Therefore, the area where plural crystal grains are overlapped is not discriminated as a crystal grain in the aforementioned identification method.
  • <<Positional Relationship Between Crystal Grain and First Unit Layer as Well as Second Unit Layer>>
  • The positional relationships between a crystal grain and the first unit layer as well as the second unit layer will be described by using FIG. 3A. FIG. 3A is a view schematically illustrating a cross-section of the first layer of the present embodiment along the film thickness direction thereof. As shown in FIG. 3A, first layer 21 has a multilayer structure in which first unit layer 1 and second unit layer 2 are alternately stacked. In FIG. 3A, a plurality of crystal grains 24 is indicated, and the boundary between crystal grains 24 is indicated as a grain boundary 25. Each crystal grain 24 can consist of the first unit layer or the second unit layer. Moreover, each crystal grain 24 can be present across one or more first unit layers and one or more second unit layers. Namely, each crystal grain 24 can have a lamellar structure with the first unit layers and the second unit layers alternately stacked.
  • <<X-ray Diffraction Spectrum>>
  • In an X-ray diffraction spectrum of the first layer, the half width of a diffraction peak derived from the (200) plane of a cubic crystal is preferably 0.2° or more and 2.0° or less. Here, the half width refers to a full width at half maximum (FWHM). According thereto, the first layer has a cubic crystal structure with fine crystal grains, enabling greater hardness of the first layer and thereby improving the wear resistance of the cutting tool. The half width of the diffraction peak derived from the (200) plane of the cubic crystal refers to the half width of a peak observed in the range of diffraction angle 2θ from 42° to 45° in an X-ray diffraction spectrum.
  • The lower limit of the aforementioned half width is preferably 0.2° or more. The upper limit of the above half width is preferably 2.0° or less from the viewpoint of improving the hardness of the first layer, more preferably 1.5° or less, and still more preferably 1.0° or less. The above half width is preferably 0.2′ or more and 2.0° or less, more preferably 0.2° or more and 1.5° or less, and still more preferably 0.2′ or more and 1.0° or less.
  • An X-ray diffraction spectrum of the first layer was measured by using a “SmartLab” (trademark) manufactured by Rigaku Corporation under the following conditions.
  • X-ray source: Cu-kα ray
  • X-ray output: 45 kV, 40 mA
  • Detector: One dimensional semiconductor detector
  • Measurement range of diffraction angle 2θ: 20° to 90°
  • Scanning speed: 10°/min
  • <<Nanoindentation Hardness of First Layer>>
  • Nanoindentation hardness H of the first layer at 25° C. is preferably 30 GPa or greater. Accordingly, the wear resistance of the cutting tool is improved. The lower limit of nanoindentation hardness H is preferably 30 GPa or greater, more preferably 34 GPa or greater, and still more preferably 38 GPa or greater. The upper limit of nanoindentation hardness H is not particularly limited, and can be set to 60 GPa or smaller from the viewpoint on manufacturing. Nanoindentation hardness H is preferably 30 GPa or greater and 60 GPa or smaller, and more preferably 34 GPa or greater and 60 GPa or smaller, and still more preferably 38 GPa or greater and 60 GPa or smaller.
  • Nanoindentation hardness H of the above first layer at 25° C. is calculated by a nanoindentation method complied with the standard procedure set forth in “ISO 14577-1:2015 Metallic materials-Instrumented indentation test for hardness and materials parameters.” A measurement apparatus that is an “ENT-1100a” manufactured by Elionix Inc,, is used. An indentation load of an indenter is 1 g, Indentation of the indenter is conducted along a cross-section of the first layer in the vertical direction (i.e., parallel to a surface of the base material) for the first layer exposed in the cross-section parallel to the normal direction of the surface of the base material.
  • The aforementioned measurement is conducted for five measurement samples, and an average value of the nanoindentation hardness obtained for each sample is taken as nanoindentation hardness of the first layer. Data that appear to be anomalous values at first glance shall be excluded.
  • It has been confirmed that there is no variation in the measurement results even though measurement points are arbitrarily selected, as long as the same cutting tool is used for measurement.
  • <<H/E in First Layer>>
  • A ratio of nanoindentation hardness H (GPa) of the first layer at 25° C. to Young's modulus E (GPa) of the first layer at 25° C., H/E, is preferably 0.070 or more. According thereto, the cutting tool can have excellent wear resistance as well as chipping resistance, thereby further improving the tool life. From the viewpoint of excellent balance between the wear resistance and chipping resistance, the H/E value is preferably 0.070 or more, more preferably 0.073 or more, and still more preferably 0.076 or more. The upper limit of H/E is not particularly limited, and can be set to 0.120 or less from the viewpoint on manufacturing. H/E is preferably 0.070 or more and 0.120 or less, more preferably 0.073 or more and 0.120 or less, and still more preferably 0.076 or more and 0.120 or less.
  • The aforementioned nanoindentation hardness H is preferably 30 GPa or greater and 50 GPa or smaller, more preferably 35 GPa or greater and 50 GPa or smaller, and still more preferably 40 GPa or greater and 50 GPa or smaller.
  • Young's modulus E is preferably 350 GPa or greater and 600 GPa or smaller, more preferably 350 GPa or greater and 550 GPa or smaller, and still more preferably 350 GPa or greater and 500 GPa or smaller. Young's modulus E is measured by the same method and under the same conditions as nanoindentation hardness H described above.
  • Embodiment 2: Method for Manufacturing Cutting Tool
  • In Embodiment 2, a method for manufacturing the cutting tool of Embodiment 1 will be described. The manufacturing method can include a step of preparing a base material and a step of forming a coating on the base material. Details of each step will be described below.
  • <<Step of Preparing Base Material>>
  • In the step of preparing a base material, a base material 10 is prepared. Base material 10 that is the base material described in Embodiment 1 can be used.
  • <<Step of Forming a Coating>>
  • In the step of forming a coating, a film 20 is formed on base material 10. In the present embodiment, a physical vapor deposition (PVD) method can be employed to form film 20. Examples of the PVD method include an Arc Ion Plating (AIP) method, a balanced magnetron sputtering (BMS) method, and an unbalanced magnetron sputtering (UBMS) method, and the like. In the present embodiment, the arc ion plating method is preferred.
  • In the AIP method, an arc discharge is generated with a target material as a cathode. This evaporates and ionizes the target material. Ions are then deposited on a surface of base material 10 to which a negative bias voltage is applied. The AIP method is superior in ionization rate of the target material.
  • A deposition apparatus used in the AIP method will be described using FIGS. 3 and 4 . As shown in FIG. 3 , a deposition apparatus 200 is equipped with a chamber 201. Chamber 201 has a gas inlet port 202 for introducing a raw material gas to chamber 201 and a gas exhaust port 203 for discharging the material gas from inside chamber 201 to an outside. Gas exhaust port 203 is connected to a vacuum pump, which is not shown in the figure. Pressure in chamber 201 is adjusted by the amount of gas introduced and discharged.
  • A rotary table 204 is disposed in chamber 201. A base material holder 205 for holding base material 10 is attached to rotary table 204, Base material holder 205 is connected to a negative electrode of a bias power supply 206. A positive electrode of bias power supply 206 is grounded.
  • As shown in FIG. 4 , a plurality of target materials 211, 212, 213, 214 is attached to side walls of chamber 201, As shown in Fig, 3, each of target materials 211 and 212 is connected to negative electrodes of direct current power supplies 221 and 222. Direct current power supplies 221 and 222 are variable power supplies, and their positive electrodes are grounded. The same is true for target materials 213 and 214, although not shown in FIG. 3 . Specific operations will be described below.
  • A base material holder 205 holds base material 10. Using a vacuum pump, chamber 201 is adjusted to the inside pressure of 1.0×10−4 Pa. While rotating rotary table 204, base material 10 is adjusted to a temperature of 500° C. by a heater (not shown) attached to deposition apparatus 200.
  • Ar gas is introduced from gas inlet port 202, and chamber 201 is adjusted to the inside pressure of 3.0 Pa. While maintaining the same pressure, power supply 206 gradually varies its voltage and is finally adjusted to −1000 V. A surface of base material 10 is then cleaned by ion bombardment treatment with Ar ions.
  • Next, a coating in the case of including second layer 22 forms second layer 22 on a surface of base material 10. For example, a TiCN layer, TiN layer, or TiCNO layer is formed on the surface of base material 10.
  • Next, first layer 21 is formed on the surface of base material 10 or on a surface of second layer 22. A sintered alloy containing Ti, Al and B is used as a target material. Each target material is set at a predetermined position, nitrogen gas is introduced from gas inlet port 202 to form first layer 21 while rotating rotary table 204. Forming conditions of first layer 21 are as follows.
  • (Forming Condition of First Layer)
  • Base material temperature: 400 to 650° C.
  • Bias voltage : −400 to −30 V
  • Arc current : 80 to 200 A
  • Reaction gas pressure: 5 to 10 Pa
  • The base material temperature, reaction gas pressure, bias voltage, and arc current are set to constant values within the ranges described above, or varied continuously within the above ranges.
  • The first unit layer and second unit layer can be appropriately formed in combinations of the methods (A) to (D) below.
  • (A) In the AIP method, a plurality of target materials (sintered alloys) having different compositions with each other is used. For example, a composition of the target material used for forming the first unit layer can be Ti60-A130-B10 and a composition of the target material used for forming the second unit layer can be Ti50-A140-B10.
  • (B) In the AIP method, bias voltage applied to base material 10 during deposition is varied within the bias voltage (−400 to −30 V) described in the forming conditions of the first layer described above.
  • (C) In the AIP method, a gas flow rate is varied. For example, the gas flow rate upon forming of the first unit layer can be set to 500 sccm to 2000 sccm, and the gas flow rate upon forming of the second unit layer can be set to 500 sccm to 2000 sccm.
  • (D) In the AIP method, base material 10 is rotated to control a rotation cycle. For example, the rotation cycle can be set to 1 rpm to 5 rpm.
  • Next, a coating in the case of including a third layer 23, for example, forms third layer 23 on a surface of first layer 21 For example, a TiC layer, TiN layer or TiCN layer is formed on the surface of first layer 21.
  • From the above, cutting tool 100 including base material 10 and coating 20 arranged on base material 10 can be manufactured.
  • Appendix 1
  • A cutting tool comprising a base material and a coating arranged on the base material, wherein
      • the coating includes a first layer;
      • the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
      • a thickness of the first unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the second unit layer is 2 nm or more and less than 50 nm;
      • a thickness of the first layer is 1.0 μm or more and 20 μm or less,
      • the first unit layer is composed of TiaAlbN, and
      • the second unit layer is composed of TidAleBfN,
        wherein

  • 0.54≤a≤0.75,

  • 0.24≤b≤0.45,

  • 0<c≤0.10,

  • a+b+c=1.00,

  • 0.44≤d≤0.65,

  • 0.34≤e≤0.55,

  • 0<f≤0.10,

  • d+e+f=1.00,

  • 0.05≤a−e≤0.20, and

  • 0.05≤e−b≤0.20 are satisfied, and
  • a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer,
  • Appendix 2
  • The cutting tool according to appendix 1, wherein
      • the first layer is composed of a plurality of crystal grains, and
      • the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
    Appendix 3
  • The cutting tool according to appendix 1 or 2, wherein in an X-ray diffraction spectrum of the first layer, a half width of a diffraction peak derived from (200) plane of a cubic crystal is 0.2″ or more and 2.0° or less.
  • Appendix 4
  • The cutting tool according to any one of appendixes 1 to 3, wherein a nanoindentation hardness H of the first layer at 25° C. is 30 GPa or greater.
  • Appendix 5
  • The cutting tool according to any one of claims 1 to 4, wherein a ratio of a nanoindentation hardness H of the first layer at 25° C. to a Young's modulus E of the first layer at 25° C., H/E, is 0.070 or more.
  • Appendix 6
  • In the cutting tool of the present disclosure, the thickness of the coating is preferably 1.0 μm or more and 25 μm or less.
  • In the cutting tool of the present disclosure, the thickness of the coating is preferably 2.0 pin or more and 16 pm or less.
  • In the cutting tool of the present disclosure, the thickness of the coating is preferably 2.0 pm or more and 16 pm or less.
  • Appendix 7
  • In the cutting tool of the present disclosure, the total number of stacking of the first unit layer and the second unit layer included in the first is preferably more than 10 and 5000 or less.
  • The above number of stacking is preferably 200 or more and 5000 or less.
  • The above number of stacking is preferably 400 or more and 2000 or less.
  • The above number of stacking is preferably 500 or more and 1000 or less.
  • Appendix 8
  • In the cutting tool of the present disclosure, the thickness of the first layer is preferably 2.0 μm or more and 16 μm or less.
  • In the cutting tool of the present disclosure, the thickness of the first layer is preferably 3.0 μm or more and 12 μm or less.
  • EXAMPLES
  • The present embodiment will be described more specifically by way of Examples. However, the present embodiment is not restricted by these Examples.
  • <Fabrication of Cutting Tool>
  • A cutting tool is fabricated as follows and a tool life was evaluated.
  • <<Samples 1 to 29, Samples 1-1 to 1-10 >>
  • A cutting insert made of cemented carbide (model number: SEMT13T3AGSR manufactured by Sumitomo Electric Hardmetal Ltd.) was prepared as a base material. The cemented carbide contains WC particles (90% by mass) and Co (10% by mass) The average particle size of the WC particle is 2 μm.
  • A coating was formed on the aforementioned base material by using a deposition apparatus having the configuration shown in FIGS. 4 and 5 . First, a surface of the base material was cleaned by ion bombardment treatment with Ar ions. The specific conditions of the ion bombardment treatment are as described in Embodiment 2.
  • Next, sintered alloys having the compositions listed in the “First unit layer” and “Second unit layer” columns of “Target material composition” in Tables 1 and 2 were prepared as target materials, For example, in Sample 1, a sintered alloy with the ratio of the numbers of atoms of Ti, Al and B, “Ti:Al:B=0.54:0.44:0.02” as the target material for forming of the first unit layer and a sintered alloy with the ratio of the numbers of atoms of Ti, Al and B, “Ti:Al:B=0.40:0.56:0.04” as the target material for forming of the second unit layer, were prepared.
  • The target materials were set at predetermined positions in the deposition apparatus. Nitrogen gas was introduced from the gas inlet port, and the first layer was formed while rotating the rotary table. The first layer forming conditions (base material temperature, bias voltage, arc current, and reaction gas pressure) for each sample are as shown in the “First layer forming conditions” column of Tables 1 and 2. A rotation speed of the rotary table was adjusted according to the film thicknesses of the first unit layer and second unit layer.
  • TABLE 1
    Upon first unit layer forming Upon second unit layer forming
    Base Base
    Target material composition material Reaction material Reaction
    Second unit temp- Bias Arc gas temp- Bias Arc gas
    Sample First unit layer layer erature voltage current pressure erature voltage current pressure
    No. Ti Al B Ti Al B ° C. V A Pa ° C. V A Pa
    1 0.54 0.44 0.02 0.40 0.56 0.04 500 100 160 5 500 100 80 5
    2 0.65 0.25 0.10 0.60 0.37 0.03 550 100 120 8 550 100 120 8
    3 0.60 0.35 0.05 0.45 0.40 0.15 450 100 120 6 450 100 120 6
    4 0.60 0.35 0.05 0.60 0.37 0.03 500 150 150 10 500 150 150 10
    5 0.61 0.32 0.07 0.60 0.37 0.03 400 100 120 8 400 100 150 8
    6 0.65 0.25 0.10 0.50 0.45 0.05 500 100 150 6 500 100 100 6
    7 0.61 0.32 0.07 0.45 0.40 0.15 550 100 150 7 550 100 15 7
    8 0.60 0.35 0.05 0.50 0.40 0.10 500 150 150 8 500 150 120 8
    9 0.54 0.44 0.02 0.50 0.45 0.05 650 300 80 6 650 300 80 6
    10 0.60 0.35 0.05 0.50 0.45 0.05 500 100 120 ? 450 100 120 7
    11 0.65 0.25 0.10 0.45 0.45 0.10 600 150 150 5 600 150 150 5
    12 0.70 0.27 0.03 0.50 0.45 0.05 600 100 150 8 600 100 150 8
    13 0.60 0.35 0.05 0.50 0.45 0.05 550 100 120 6 550 100 150 6
    14 0.60 0.35 0.05 0.50 0.45 0.05 400 50 200 10 400 50 120 10
    15 0.70 0.27 0.03 0.60 0.37 0.03 500 100 120 8 500 100 120 8
    16 0.70 0.27 0.03 0.60 0.37 0.03 550 100 180 5 550 100 180 5
    17 0.60 0.35 0.05 0.50 0.40 0.10 450 50 120 7 450 50 120 7
    18 0.70 0.22 0.08 0.50 0.45 0.05 650 400 120 7 650 400 150 7
    19 0.60 0.35 0.05 0.50 0.45 0.05 450 100 150 9 450 100 150 9
    20 0.61 0.32 0.07 0.50 0.45 1.05 400 100 120 5 400 100 150 5
    21 0.55 0.30 0.15 0.45 0.40 0.15 550 30 120 7 550 30 180 7
  • TABLE 2
    Target material composition Upon first unit layer forming Upon second unit layer forming
    Second unit Base material Bias Arc Reaction Base material Bias Arc Reaction
    Sample First unit layer layer temperature voltage current gas pressure temperature voltage current gas pressure
    No. Ti Al B Ti Al B ° C. V A Pa ° C. V A Pa
    22 0.60 0.35 0.05 0.50 0.45 0.05 500 100 200 10 500 100 80 10
    23 0.61 0.32 0.07 0,60 0.30 0.10 400 100 100 8 400 100 150 8
    24 0.60 0.35 0.05 0.50 0.45 0.05 550 150 150 5 550 150 150 5
    25 0.54 0.44 0.02 0.50 0.45 0.05 450 100 120 7 450 100 100 7
    26 0.65 0.25 0.10 0.50 0.40 0.10 550 150 150 10 550 150 150 10
    27 0.70 0.27 0.03 0.60 0.37 0.03 400 100 120 5 450 100 120 5
    28 0.65 0.25 0.10 0,50 0.45 0.05 500 100 150 7 500 100 100 7
    29 0.60 0.35 0.05 0.50 0.45 0.05 600 200 150 5 600 200 150 5
    1-1 0.54 0.44 0.02 0.40 0.56 0.04 450 100 150 8 450 100 150 8
    1-2 0.77 0.20 0.03 0.60 0.37 0.03 500 100 150 5 500 100 100 5
    1-3 0.55 0.30 0.15 0.45 0.40 0.15 500 50 200 5 500 50 200 5
    14 0.65 0.35 0.00 0.50 0.50 0.00 450 150 120 10 450 150 120 10
    1-5 0.65 0.25 0.10 0.60 0.30 0.10 400 50 150 6 400 50 150 6
    1-6 0.65 0.25 0.10 0.45 0.45 0.10 600 400 100 7 600 400 150 7
    1-7 0.70 0.22 0.08 0.50 0.40 0.10 450 200 80 7 450 200 80 7
    1-8 0.65 0.25 0.10 0,45 0.40 0.15 650 30 200 7 650 30 200 7
    1-9 0.50 0.44 0.06 0.45 0.45 0.10 550 100 120 8 550 100 150 8
    1-10 0.50 0.45 0.05 0.50 3.45 0.05 500 200 150 9 500 200 150 9
  • <Evaluation> <<Composition of Coating>>
  • The coating of each sample was measured regarding compositions of the first unit layer and second unit layer, the thickness and the number of stacking of the first unit layer, the thickness and the number of stacking of the second unit layer, the thickness and the number of stacking of the first layer, the percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron (denoted as the “Ti content in First layer” in Tables 5 and 6) in the first layer, the maximum value of diameter D of the largest inscribed circle of the crystal grain in the first layer (denoted as “Diameter of largest inscribed circle D” in Tables 5 and 6), the half width of a diffraction peak derived from the (200) plane of the cubic crystal in a X-ray diffraction spectrum of the first layer (denoted as “XRD half width” in Tables 5 and 6), nanoindentation hardness H of the first layer (denoted as “Hardness H” in Tables 5 and 6), and Young's modulus E of the first layer. The measurement methods for each item is as described in Embodiment 1. Moreover, HIE was calculated based on the measured values of nanoindentation hardness H and Young's modulus E of the first layer. The results are shown in Tables 3 to 6.
  • TABLE 3
    First unit layer Second unit layer First layer
    First unit layer Second unit layer Thick- Number Thick- Number Thick- Number
    Sample composition composition ness of ness of ness of
    No. a b c d e f a − d e − b (nm) stacking (nm) stacking (μm) stacking
    1 0.54 0.45 0.01 0.44 0.55 0.01 0.10 0.10 15 261 8 261 6.0 522
    2 0.68 0.25 0.07 0.62 0.36 0.02 0.06 0.11 20 200 20 200 8.0 400
    3 0.64 0.34 0.01 0.51 0.39 0.10 0.13 0.05 15 167 15 167 5.0 334
    4 0.66 0.32 0.02 0.59 0.40 0.01 0.07 0.08 30 177 32 177 11.0 354
    5 0.63 0.32 0.06 0.57 0.40 0.03 0.06 0.08 12 111 15 111 3.0 222
    6 0.69 0.27 0.04 0.50 0.46 0.04 0.19 0.19 26 273 18 273 12.0 546
    7 0.64 0.30 0.06 0.52 0.39 0.09 0.12 0.09 7 267 8 267 4.0 534
    8 0.61 0.36 0.03 0.52 0.41 0.07 0.09 0.05 35 79 28 79 5.0 158
    9 0.56 0.42 0.02 0.51 0.47 0.02 0.05 0.05 2 250 2 250 1.0 500
    10 0.60 0.35 0.05 0.48 0.51 0.02 0.12 0.16 49 200 49 200 20.0 400
    11 0.68 0.26 0.06 0.49 0.46 0.05 0.19 0.20 24 160 26 160 8.0 320
    12 0.72 0.27 0.01 0.53 0.44 0.03 0.19 0.17 11 391 12 391 9,0 782
    13 0.63 0.33 0.04 0.54 0.44 0.02 0.08 0.11 15 167 21 167 6.0 334
    14 0.67 0.28 0.05 0.53 0.43 0.04 0.14 0.15 46 70 25 70 5.0 140
    15 0.75 0.24 0.02 0.6 0.36 0.03 0.14 0.12 9 556 9 556 10.0 1112
    16 0.74 0.25 0.01 0.59 0.38 0.02 0.15 0.13 18 500 16 500 17.0 1000
    17 0.64 0.32 0.05 0.53 0.42 0.05 0.11 0.11 4 333 5 333 3.0 666
    18 0.69 0.27 0.04 0.56 0.40 0.04 0.13 0.13 31 74 37 74 5.0 148
    19 0.62 0.35 0.03 0.55 0.42 0.03 0.07 0.07 11 450 C33 450 9.0 900
    20 0.66 0.30 0.04 0.50 0.47 0.03 0.16 0.17 35 232 47 232 19.0 464
  • TABLE 4
    First unit layer Second unit layer First unit layer Second unit layer First layer
    Sample composition composition Thickness Number of Thickness Number of Thickness Number of
    No. a b c d e f a − d e − b (nm) stacking (nm) stacking (μm) stacking
    21 0.57 0.33 0.10 0.48 0.43 0.10 0.09 0.09 12 194 19 194 6.0 388
    22 0.66 0.32 0.03 0.54 0.43 0.03 0.11 0.11 31 116 12 116 5.0 232
    23 0.66 0.28 0.06 0.60 0.35 0.06 0.06 0.07 8 682 14 682 15.0 1364
    24 0.64 0.34 0.03 0.53 0.44 0.03 0.11 0.11 22 85 25 85 4.0 170
    25 0.56 0.42 0.02 0.47 0.51 0.02 0.09 0.09 5 1500 3 1500 12.0 3000
    26 0.61 0.30 0.08 0.51 0.41 0.08 0.11 0.11 11 857 10 857 18.0 1714
    27 0.74 0.25 0.01 0.64 0.35 0.01 0.10 0.10 8 467 7 467 7.0 934
    28 0.68 0.28 0.04 0.49 0.47 0.04 0.19 0.19 27 217 19 217 10.0 434
    29 0.61 0.36 0.03 0.51 0.47 0.03 0.10 0.10 13 250 15 250 7.0 500
    1-1 0.53 0.45 0.02 0.43 0.55 0.02 0.10 0.10 15 241 14 241 7.0 482
    1-2 0.78 0.20 0.03 0.67 0.31 0.03 0.11 0.11 18 167 12 167 5.0 334
    1-3 0.56 0.32 0.12 0.47 0.41 0.12 0.09 0.09 22 190 20 190 8.0 380
    1-4 0.64 0.36 0.00 0.55 0.45 0.00 0.09 0.09 10 316 9 316 6.0 632
    1-5 0.65 0.28 0.07 0.61 0.32 0.07 0.04 0.04 41 157 29 157 11.0 314
    1-6 0.66 0.29 0.05 0.44 0.51 0.05 0.22 0.22 8 250 12 250 5.0 500
    1-7 0.71 0.23 0.06 0.53 0.41 0.06 0.18 0.18 1 250 1 250 0.5 500
    1-8 0.60 0.31 0.09 0.50 0.41 0.09 0.10 0.10 60 182 61 182 22.0 364
    1-9 0.53 0.42 0.05 0.43 0.52 0.05 0.10 0.10 13 321 15 321 9.0 642
    1-10 0.55 0.42 0.03 0.55 0.42 0.03 0.00 0.00 63 32 61 32 4.0 64
  • TABLE 5
    First layer
    Diameter of Young’s Cutting test 1 Cutting test 2
    Sample Ti content largest inscribed XRD half Hardness modulus Cutting time Cutting time
    No. (%) circle D (nm) width (°) H (GPa) E (GPa) H/E (minutes) (minutes)
    1 51 33 0.5 35 482 0.073 29 15
    2 65 21 0.8 33 439 0.075 33 15
    3 58 17 1 31 392 0.079 25 21
    4 63 31 0.6 34 466 0.073 36 12
    5 59 29 0.6 32 418 0.077 25 19
    6 61 18 0.9 37 487 0.076 39 18
    7 58 41 0.5 32 387 0.083 24 23
    8 57 27 0.7 41 518 0.079 30 19
    9 54 15 0.9 40 562 0.071 27 9
    10 54 20 0.9 39 533 0.073 42 9
    11 58 12 1.6 37 511 0.072 36 15
    12 62 20 0.9 33 426 0.077 34 16
    13 58 42 0.5 39 533 0.073 33 17
    14 62 50 0.4 31 409 0.076 26 18
    15 88 35 0.5 32 441 0.073 35 14
    18 67 57 0.3 38 555 0.068 38 9
    17 58 112 0.2 29 430 0.067 25 13
    18 62 9 2 38 539 0.071 31 15
    19 59 30 0.5 33 467 0.071 35 13
    20 57 241 0.1 34 491 0.069 36 9
    21 51 6 2.2 29 401 0.072 26 15
    22 62 46 0.4 30 422 0.071 25 16
  • TABLE 6
    First layer
    Diameter of Hardness Young’s Cutting test 1 Cutting test 2
    Sample Ti content largest inscribed XRD half H modulus E Cutting time Cutting time
    No. (%) circle D (nm) width (°) (GPa) (GPa) H/E (minutes) (minutes)
    23 63 25 0.7 37 509 0.073 39 11
    24 58 35 0,6 29 402 0.072 24 13
    25 53 13 1.5 33 471 0.070 36 12
    26 56 21 0.8 38 535 0.071 41 10
    27 69 12 1.6 33 481 0.069 33 12
    28 60 29 0.6 28 404 0.069 28 13
    29 56 221 0.1 29 412 0.070 27 14
    1-1 48 96 0.2 29 471 0.062 13 3
    1-2 74 78 0.2 28 396 0.071 16 6
    1-3 52 7 2.1 22 361 0.061 11 2
    1-4 60 239 0.1 29 526 0.055 15 4
    1-5 63 23 0.8 30 451 0.067 16 6
    1-6 53 31 0.5 38 512 0.074 16 5
    1-7 62 32 0.5 36 472 0.076 9 5
    1-8 55 48 0.3 33 467 0.071 32 1
    1-9 48 49 0.3 28 428 0.065 15 6
    1-10 55 27 0.6 32 477 0.067 15 2
  • <<Cutting Test 1>>
  • A cutting test was carried out by using the cutting tool of each sample under the following conditions, and a cutting time (minutes) until the width of crater wear reached 0.3 mm or more was measured. The cutting time longer than 24 minutes is determined that the cutting tool has excellent wear resistance. The results are shown in the “Cutting test 1” column of Tables 5 and 6.
  • (Cutting Conditions)
  • Workpiece: Stainless steel
  • Cutting speed: 250 m/min
  • Feed rate: 0.1 mm/t
  • Depth of cut: 1.0 mm
  • Dry cutting
  • Center cut
  • The above cutting conditions correspond to those for stainless steel milling (high-speed, low-feed machining).
  • <<Cutting Test 2>>
  • A cutting test was carried out by using the cutting tool of each sample under the following conditions, and a cutting time (minutes) until the width of flank wear reached mm or more was measured. The cutting time longer than 9 minutes is determined that the cutting tool has excellent chipping resistance. The results are shown in the “Cutting test 2” column of Tables 5 and 6.
  • (Cutting Conditions)
  • Workpiece: Stainless steel
  • Cutting speed: 100 m/min
  • Feed rate: 0.5 mm/t
  • Depth of cut: 2.0 mm
  • Dry cutting
  • Center cut
  • The above cutting conditions correspond to those for stainless steel milling (low-speed, high-feed machining).
  • <Considerations>
  • The cutting tools of Samples 1 to 29 correspond to Examples. Samples 1 to 29 (Examples) were confirmed to have excellent wear resistance and chipping resistance and long tool lives.
  • The cutting tools of Sample 1-1 to Sample 1-10 correspond to Comparative Examples. The first unit layer and the second unit layer have the same composition in Sample 1-10. Namely, Sample 1-10 has a single layer with uniform composition. Sample 1-1 to Sample 1-10 were confirmed to have insufficient wear resistance and/or chipping resistance and insufficient tool lives.
  • The embodiments and Examples of the present disclosure have been explained as described above, however appropriate combinations of each aforementioned embodiment and the configurations of Examples as well as variations thereof in various ways, have been contemplated from the beginning. The embodiments and Examples disclosed herein are illustrative in all respects and should be considered not restrictive. The scope of the present disclosure is indicated by the claims, not by the aforementioned embodiments and Examples, and is intended to include the meaning equivalent to the scope of the claims and all modifications within the scope.
  • REFERENCE SIGNS LIST
  • 1 first unit layer, 2 second unit layer, 10 base material, 20 coating, 21 first layer, 22 second layer, 23 third layer, 24, 24 a, 24 b, and 24 c crystal grains, 25 grain boundary, atom, 100 cutting tool, 200 deposition apparatus, 201 chamber, 202 gas inlet port, 203 gas exhaust port, 204 rotary table, 205 base material holder, 206 bias power supply, 211, 212, 213, and 214 target materials, 221 and 222 direct current power supply.

Claims (5)

1. A cutting tool comprising a base material and a coating arranged on the base material, wherein
the coating comprises a first layer;
the first layer has a multilayer structure in which a first unit layer and a second unit layer are alternately stacked;
a thickness of the first unit layer is 2 nm or more and less than 50 nm;
a thickness of the second unit layer is 2 nm or more and less than 50 nm;
a thickness of the first layer is 1.0 μm or more and 20 μm or less,
the first unit layer is composed of TiaAlbBcN, and
the second unit layer is composed of TidAleBfN,
wherein

0.54≤a≤0.75,

0.24≤b≤0.45,

0<c≤0.10,

a+b+c=1.00,

0.44≤d≤0.65,

0.34≤e≤0.55,

0<f≤0.10,

d+e+f=1.00,

0.05≤a−d≤0.20, and

0.05≤e−b≤0.20 are satisfied, and
a percentage of the number of atoms of titanium to the total number of atoms of titanium, aluminum and boron is 50% or more in the first layer.
2. The cutting tool according to claim 1, wherein
the first layer is composed of a plurality of crystal grains, and
the diameter of the largest inscribed circle of the crystal grain is 50 nm or smaller.
3. The cutting tool according to claim 1, wherein in an X-ray diffraction spectrum of the first layer, a half width of a diffraction peak derived from (200) plane of a cubic crystal is 0.2° or more and 2.0° or less.
4. The cutting tool according to claim 1, wherein a nanoindentation hardness H of the first layer at 25° C. is 30 GPa or greater.
5. The cutting tool according to claim 1, wherein a ratio of a nanoindentation hardness H(GPa) of the first layer at 25° C. to a Young's modulus E(GPa) of the first layer at 25° C., H/E, is 0.070 or more.
US18/018,890 2022-06-15 2022-06-15 Cutting tool Abandoned US20230405687A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2022/023996 WO2023243007A1 (en) 2022-06-15 2022-06-15 Cutting tool

Publications (1)

Publication Number Publication Date
US20230405687A1 true US20230405687A1 (en) 2023-12-21

Family

ID=87882213

Family Applications (1)

Application Number Title Priority Date Filing Date
US18/018,890 Abandoned US20230405687A1 (en) 2022-06-15 2022-06-15 Cutting tool

Country Status (3)

Country Link
US (1) US20230405687A1 (en)
JP (1) JP7338827B1 (en)
WO (1) WO2023243007A1 (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180099335A1 (en) * 2016-03-28 2018-04-12 Sumitomo Electric Hardmetal Corp. Surface-coated cutting tool and method for manufacturing same
US20190247930A1 (en) * 2016-11-29 2019-08-15 Sumitomo Electric Hardmetal Corp. Surface-coated cutting tool
US20200298316A1 (en) * 2016-03-30 2020-09-24 Mitsubishi Hitachi Tool Engineering, Ltd. Coated cutting tool

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007038378A (en) * 2005-08-05 2007-02-15 Mitsubishi Materials Corp Surface-coated cemented-carbide cutting tool with hard coating layer capable of showing excellent chipping resistance in high speed cutting of difficult-to-cut material
JP5440346B2 (en) 2010-04-15 2014-03-12 三菱マテリアル株式会社 Surface coated cutting tool
JP5594577B2 (en) 2010-04-20 2014-09-24 三菱マテリアル株式会社 Surface coated cutting tool
EP3769869A4 (en) 2018-03-22 2021-12-29 Sumitomo Electric Hardmetal Corp. Surface coated cutting tool and method for manufacturing same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180099335A1 (en) * 2016-03-28 2018-04-12 Sumitomo Electric Hardmetal Corp. Surface-coated cutting tool and method for manufacturing same
US20200298316A1 (en) * 2016-03-30 2020-09-24 Mitsubishi Hitachi Tool Engineering, Ltd. Coated cutting tool
US20190247930A1 (en) * 2016-11-29 2019-08-15 Sumitomo Electric Hardmetal Corp. Surface-coated cutting tool

Also Published As

Publication number Publication date
JP7338827B1 (en) 2023-09-05
JPWO2023243007A1 (en) 2023-12-21
WO2023243007A1 (en) 2023-12-21

Similar Documents

Publication Publication Date Title
JP6268530B2 (en) Surface coated cutting tool with excellent chipping resistance due to hard coating layer
CN104789938A (en) Surface coating cutting tool hard coating layer of which gives play to excellent anti-tipping performance
KR20220024491A (en) Method of making coated cutting tools and coated cutting tools
US10994341B2 (en) Surface-coated cutting tool and method for manufacturing same
JP2021030356A (en) Surface-coated cutting tool
US20230405687A1 (en) Cutting tool
US11938548B2 (en) Cutting tool
US20220297197A1 (en) Coated cutting tool
JP2006116621A (en) Surface-coated cermet cutting tool with hard coating layer exerting excellent chipping resistance in high-speed intermittent cutting
JP7226688B2 (en) Cutting tools
JP7486045B2 (en) Surface-coated cutting tools
WO2022239139A1 (en) Cutting tool
US11524339B2 (en) Cutting tool
WO2022176230A1 (en) Surface-coated cutting tool
WO2024048757A1 (en) Coated tool and cutting tool
JP2019098502A (en) Surface-coated cutting tool having hard coating layer excellent in thermal cracking resistance
JP7418714B2 (en) coated cutting tools
JP6743350B2 (en) Cutting tools
JP7353591B2 (en) coated cutting tools
WO2020213263A1 (en) Cutting tool
JP2024005014A (en) Cutting tool
CN117222775A (en) Coated cutting tool
JP2024005015A (en) Cutting tool
JP2023000875A (en) Coated cutting tool
JP2021146419A (en) Surface-coated cutting tool

Legal Events

Date Code Title Description
AS Assignment

Owner name: SUMITOMO ELECTRIC HARDMETAL CORP., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SUZUKI, YUTA;IMAMURA, SHINYA;SIGNING DATES FROM 20221117 TO 20221129;REEL/FRAME:062547/0520

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION